Bravo Ana Luisa, Sigala Juan Carlos, Le Borgne Sylvie, Morales Marcia
División de Ciencias Naturales e Ingeniería, Universidad Autónoma Metropolitana Cuajimalpa, Avenida Vasco de Quiroga 4871, Colonia Santa Fe, Delegación Cuajimalpa de Morelos, 05348, México, D.F., Mexico,
Biotechnol Lett. 2015 Apr;37(4):807-14. doi: 10.1007/s10529-014-1737-5. Epub 2014 Nov 29.
Pseudomonas citronellolis UAM-Ps1 co-metabolically transforms methyl tert-butyl ether (MTBE) to tert-butyl alcohol with n-pentane (2.6 mM), n-octane (1.5 mM) or dicyclopropylketone (DCPK) (4.4 mM), a gratuitous inducer of alkane hydroxylase (AlkB) activity. The reverse transcription quantitative real-time PCR was used to quantify the alkane monooxygenase (alkB) gene expression. The alkB gene was expressed in the presence of n-alkanes and DCPK and MTBE oxidation occurred only in cultures when alkB was transcribed. A correlation between the number of alkB transcripts and MTBE consumption was found (ΜΤΒΕ consumption in μmol = 1.44e(-13) x DNA copies, R(2) = 0.99) when MTBE (0.84 mM) was added. Furthermore, alkB was cloned and expressed into Escherichia coli and the recombinant AlkB had a molecular weight of 42 kDa. This is the first report where the expression of alkB is related to the co-metabolic oxidation of MTBE.
香茅假单胞菌UAM-Ps1能利用正戊烷(2.6 mM)、正辛烷(1.5 mM)或二环丙基甲酮(DCPK)(4.4 mM)作为烷烃羟化酶(AlkB)活性的诱导剂,将甲基叔丁基醚(MTBE)共代谢转化为叔丁醇。采用逆转录定量实时PCR对烷烃单加氧酶(alkB)基因表达进行定量分析。alkB基因在正构烷烃、DCPK存在时表达,且只有在alkB转录的培养物中才会发生MTBE氧化。添加MTBE(0.84 mM)时,发现alkB转录本数量与MTBE消耗之间存在相关性(MTBE消耗以μmol计 = 1.44e(-13)×DNA拷贝数,R(2)=0.99)。此外,alkB被克隆并在大肠杆菌中表达,重组AlkB的分子量为42 kDa。这是首次报道alkB的表达与MTBE的共代谢氧化有关。